Primary Device ID | 00810019244285 |
NIH Device Record Key | 5ba5c7a8-68f0-4dae-8213-2077ca4103ad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bite Impression Coping (Mini) |
Version Model Number | ETBICM4620 |
Company DUNS | 796083090 |
Company Name | HIOSSEN, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810019244285 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-04 |
Device Publish Date | 2021-07-27 |
00810019244353 | ETBICM4651 |
00810019244346 | ETBICM4650 |
00810019244339 | ETBICM4641 |
00810019244322 | ETBICM4640 |
00810019244315 | ETBICM4631 |
00810019244308 | ETBICM4630 |
00810019244292 | ETBICM4621 |
00810019244285 | ETBICM4620 |
00810019244278 | ETBICM4451 |
00810019244261 | ETBICM4450 |
00810019244254 | ETBICM4441 |
00810019244247 | ETBICM4440 |
00810019244230 | ETBICM4431 |
00810019244223 | ETBICM4430 |
00810019244216 | ETBICM4421 |
00810019244209 | ETBICM4420 |
00810019247835 | EKBIC4641 |